Interesting facts
Interesting Facts About 2-(dimethylamino)ethyl 2-(1-hydroxycyclopentyl)-2-phenyl-acetate
This intriguing compound, 2-(dimethylamino)ethyl 2-(1-hydroxycyclopentyl)-2-phenyl-acetate, is notable for several compelling reasons:
- Pharmacological Potential: This compound is often explored for its potential therapeutic uses, particularly in the field of pharmaceutical chemistry. Its unique structure allows for interactions that could be beneficial in developing new medications.
- Structural Composition: The presence of both a dimethylamino group and a phenyl group makes this compound interesting. The combination leads to diverse electronic properties, influencing its reactivity and interactions with biological systems.
- Hydroxycyclopentyl Moiety: The inclusion of a cyclopentyl ring presents a stereochemical aspect that can greatly affect the molecule's spatial configuration and how it fits into biological targets. This structural feature may contribute to specific binding affinities in receptors.
- Versatile Applications: Due to its properties, this compound could have roles beyond pharmaceuticals, including agricultural or industrial applications where similar chemical characteristics are valued.
- Research Opportunities: The complexity of the compound invites scientists to explore various research angles, such as synthetic routes, mechanistic studies, and the compound's interactions at the molecular level, engaging students and researchers alike.
In conclusion, 2-(dimethylamino)ethyl 2-(1-hydroxycyclopentyl)-2-phenyl-acetate represents a remarkable intersection of organic chemistry and pharmacology, opening pathways for innovation and deeper understanding in the synthesis and application of complex organic molecules. As research progresses, the full potential of this compound continues to reveal itself, promising exciting avenues for exploration.
Synonyms
cyclopentolate
512-15-2
Ciclopentolato
Cyclopentolatum
Cyclopentylate
Cyclogyl
2-(dimethylamino)ethyl 2-(1-hydroxycyclopentyl)-2-phenylacetate
Bell Pentolate
Cyclopentolatum [INN-Latin]
Ciclopentolato [INN-Spanish]
(+-)-cyclopentolate
UNII-I76F4SHP7J
EINECS 208-136-4
I76F4SHP7J
CHEBI:4024
2-(Dimethylamino)ethyl 1-hydroxy-alpha-phenylcyclopentaneacetate
Cyclopentolate (INN)
1-hydroxy-alpha-phenylcyclopentaneacetic acid 2-(dimethylamino)ethyl ester
alpha-(1-hydroxycyclopentyl)benzeneacetic acid 2-(dimethylamino)ethyl ester
Benzeneacetic acid, .alpha.-(1-hydroxycyclopentyl)-, 2-(dimethylamino)ethyl ester
Benzeneacetic acid, alpha-(1-hydroxycyclopentyl)-, 2-(dimethylamino)ethyl ester
beta-dimethylaminoethyl (1-hydroxycyclopentyl)phenylacetate
2-(Dimethylamino)ethyl (1-hydroxycyclopentyl)(phenyl)acetate
beta-(Dimethylamino)ethyl (1-hydroxycyclopentyl)phenylacetate
DTXSID3048528
2-Dimethylaminoethyl 2-(1-hydroxycyclopentyl)-2-phenylacetat
2-phenyl-2-(1-hydroxycyclopentyl)ethanoic acid beta-(dimethylamino)ethyl ester
Tsiklopentolat;Cyclogyl;DL-Cyclopentolate
Cyclopentoiate
Diopentolate
CYCLOPENTOLATE [INN]
Cyclopentolatum (INN-Latin)
Ciclopentolato (INN-Spanish)
Cyclopentolate [INN:BAN]
Bell Pentolate (TN)
cyclo-pentolatum
Cyclogyl (Salt/Mix)
Mydrilate (Salt/Mix)
Spectrum_000856
(+/-)-cyclopentolate
Prestwick0_001095
Prestwick1_001095
Prestwick2_001095
Prestwick3_001095
Spectrum2_001122
Spectrum3_000369
Spectrum4_000303
Spectrum5_000793
CYCLOPENTOLATE [MI]
BSPBio_001170
BSPBio_002097
KBioGR_000886
KBioSS_001336
CYCLOPENTOLATE [VANDF]
DivK1c_000610
SCHEMBL132500
SPBio_000983
SPBio_003055
BPBio1_001288
GTPL7153
CYCLOPENTOLATE [WHO-DD]
CHEMBL1201338
DTXCID4027995
BDBM82375
KBio1_000610
KBio2_001336
KBio2_003904
KBio2_006472
KBio3_001317
S01FA04
NINDS_000610
BCP21334
NSC_2905
MFCD00599448
STL430452
AKOS015962137
DB00979
FC61687
IDI1_000610
Cyclopentolatum; Cyclogyl; Cyclopentylate
NCGC00018213-02
AC-15991
AS-16057
CAS_512-15-2
DA-72483
SBI-0051324.P003
AB00053445
NS00009832
C06932
D07759
H10434
AB00053445_12
EN300-7359577
L000802
Q867332
BRD-A77291778-003-05-5
BRD-A77291778-003-15-4
BRD-A77291778-003-22-0
.beta.-(Dimethylamino)ethyl (1-hydroxycyclopentyl)phenylacetate
2-(Dimethylamino)ethyl (1-hydroxycyclopentyl)(phenyl)acetate #
2-Dimethylaminoethyl 1-hydroxy-.alpha.-phenylcyclopentaneacetate
1-Hydroxy-.alpha.-phenylcyclopentaneacetic acid, 2-(dimethylamino)ethyl ester
2-(DIMETHYLAMINO)ETHYL (+/-)-1-HYDROXY-.ALPHA.-PHENYLCYCLOPENTANEACETATE
2-(DIMETHYLAMINO)ETHYL (+/-)-1-HYDROXY-alpha-PHENYLCYCLOPENTANEACETATE
Cyclopentaneacetic acid, 1-hydroxy-.alpha.-phenyl-, 2-(dimethylamino)ethyl ester
2-Dimethylaminoethyl 2-(1-Hydroxycyclopentyl)-2-Phenyl-Acetate;2-(1-Hydroxycyclopentyl)-2-Phenyl-Acetic Acid 2-Dimethylaminoethyl Es ter
208-136-4
Solubility of 2-(dimethylamino)ethyl 2-(1-hydroxycyclopentyl)-2-phenyl-acetate
The solubility of 2-(dimethylamino)ethyl 2-(1-hydroxycyclopentyl)-2-phenyl-acetate (C19H25NO3) can be influenced by several factors, including polarity, functional groups, and environment. Understanding these elements can help assess how this compound behaves in different solvents.
Factors Affecting Solubility:
In general, compounds similar to 2-(dimethylamino)ethyl 2-(1-hydroxycyclopentyl)-2-phenyl-acetate demonstrate varying degrees of solubility based on these influencing factors.
To summarize, the solubility of this compound is likely moderate, exhibiting higher solubility in polar solvents due to the presence of the hydroxyl group, while also being soluble in organic solvents because of its hydrophobic portions.